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Role of miR-29c in modulating the paracrine crosstalk between eso | 16420
Chemotherapy: Open Access

Chemotherapy: Open Access
Open Access

ISSN: 2167-7700

+44 1223 790975

Role of miR-29c in modulating the paracrine crosstalk between esophageal cancer cells and stromal fibroblasts in the tumor microenvironment


International Conference on Antimicrobial Agents and Chemotherapy

August 04-06, 2015 Valencia, Spain

Wen Wen Xu, Bin Li and Annie L M Cheung

Scientific Tracks Abstracts: Chemotherapy

Abstract :

Esophageal cancer is the 8th most common cancer worldwide, with more than 480,000 new cases diagnosed every year. Angiogenesis is a major clinical feature of aggressive esophageal squamous cell carcinoma (ESCC). However, understanding of the cellular and molecular mechanisms of tumor angiogenesis remains poor. Our results demonstrated that insulin-like growth factor 2 (IGF2) secreted by ESCC cells could activate stromal fibroblasts in a paracrine manner, stimulating them to migrate and produce vascular endothelial growth factor (VEGF). Knockdown of IGF2 or neutralization of IGF2 using specific antibody greatly abrogated this effect. In silico target prediction algorithms and RT-PCR were used to screen for microRNAs that might mediate the regulation of IGF2 on VEGF. Amongst the potential candidates, miR-29c was found to satisfy the criteria of having conserved seed regions that perfectly matched with the 3�??UTR of VEGF and being downregulated by IGF2. Gain and loss of function studies showed that miR- 29c negatively regulated the expression of VEGF in normal fibroblasts and mediated the regulation of IGF2 on VEGF. Results from luciferase reporter assay indicated direct binding of miR-29c to the 3�??UTR of VEGF. More importantly, analysis of GEO datasets showed stromal VEGF to be a prognostic biomarker in breast cancer, and its potential in ESCC prognosis will be evaluated. Taken together, these data provide the first evidence showing that the IGF2/miR-29c/VEGF regulatory axis may have an important role in tumor progression.

Biography :

Wen Wen Xu is a final year PhD student in the University of Hong Kong. She got her MPhil degree from The Chinese University of Hong Kong in 2012. Her current research interests include: 1) Role of Id1 in the regulation of tumor micro-environment and macro-environment; 2) Cellular and molecular mechanisms of tumor angiogenesis and potential targeted therapy. She was honored with many prestigious international and local awards and scholarships, including 2013 UK National Cancer Research Institute prize award, 21st Hong Kong International Cancer Congress Best Poster prize, Mary Sun Medical Scholarships, YS and Christabel Lung Postgraduate Scholarship.

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